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Discovery of a Novel, Orally Efficacious Liver X Receptor (LXR) β Agonist

Authors :
Deepak S. Lala
Paula Krosky
Kerri Lipinski
Colin M. Tice
Ya-Jun Zheng
Lamont Howard
Richard Gregg
Paul B. Noto
Yi Zhao
Kristi Fan
David A. Claremon
Zhongren Wu
Andrew W. Hardy
Rebecca Van Orden
Jing Zhou
Gerard McGeehan
Joan Guo
Cheng-Guo Dong
Stephen D. Lotesta
Geeta Kandpal
Jun Shimada
Zhijie Liu
Katerina Leftheris
Shi Meng
Suresh B. Singh
Guozhou Chen
Linghang Zhuang
Brian M. McKeever
Peter Lindblom
Yuri Bukhtiyarov
Wei Zhao
Source :
Journal of medicinal chemistry. 59(7)
Publication Year :
2016

Abstract

This article describes the application of Contour to the design and discovery of a novel, potent, orally efficacious liver X receptor β (LXRβ) agonist (17). Contour technology is a structure-based drug design platform that generates molecules using a context perceptive growth algorithm guided by a contact sensitive scoring function. The growth engine uses binding site perception and programmable growth capability to create drug-like molecules by assembling fragments that naturally complement hydrophilic and hydrophobic features of the protein binding site. Starting with a crystal structure of LXRβ and a docked 2-(methylsulfonyl)benzyl alcohol fragment (6), Contour was used to design agonists containing a piperazine core. Compound 17 binds to LXRβ with high affinity and to LXRα to a lesser extent, and induces the expression of LXR target genes in vitro and in vivo. This molecule served as a starting point for further optimization and generation of a candidate which is currently in human clinical trials for treating atopic dermatitis.

Details

ISSN :
15204804
Volume :
59
Issue :
7
Database :
OpenAIRE
Journal :
Journal of medicinal chemistry
Accession number :
edsair.doi.dedup.....72847825e5e910bcb4d0f464f422727e